120 English-speaking jobs in Walloon Brabant

Contribute to regulatory bioanalysis activities supporting new therapy development. Perform routine analysis on samples and validate bioanalytical methods in a GLP-compliant environment.

Global Physical Asset Manager for biopharma equipment. Oversees lifecycle performance, ensuring safety, compliance, and efficiency. Develops asset management strategies across research, development, and manufacturing.

Leads a team of network engineers, delivering network projects and ensuring secure, scalable network operations across corporate, research, and manufacturing environments.

Junior Bioanalytical Scientist to develop PK bioanalytical methods, primarily LBA, supporting drug candidates in clinical development.

Lead the consolidation and reporting function, ensuring accuracy and timeliness of group accounts under IFRS. Drive harmonization of accounting practices and optimize the consolidation system.

The Vendor Quality Lead & QP provides QA expertise for Global Vendors engaged in GMP manufacturing. Responsibilities include managing vendor quality agreements, reviewing deviations and investigations, and ensuring timely completion of Product Quality Reviews. The role requires a Master's degree in a relevant scientific discipline, eight years of QA experience in the pharmaceutical sector, and a valid Qualified Person (QP) Certification. Fluent English is required.

Leads the identification, development, and implementation of drug delivery systems from research to commercialization. Ensures delivery solutions are patient-centric and aligned with UCB product strategies. Collaborates with cross-functional teams to anticipate needs, align stakeholders, and ensure continuity.

Develop, implement, and lead Pharmacometrics AI/ML strategy to support drug development. Evaluate and implement emerging technologies for quantitative clinical pharmacology and pharmacometrics applications. Perform AI/ML, population PK/PD, exposure-response modeling, and clinical trial simulations.

Designs customer-centric cryptographic architectures, analyzes security needs, and defines optimal solutions. Leads system specification, design, and Make/Team/Buy decisions, collaborating with hardware, software, security, and QA teams. Acts as the technical authority on cryptography, driving innovation, risk assessments, and best practices.

Lead and manage a team of embedded software engineers, ensuring the successful delivery of high-quality, reliable, and secure embedded software. Oversee the estimation and planning of development tasks, ensuring project deadlines are met. Drive continuous improvement initiatives within the team and the broader organization.

Design and maintain high quality digital solutions in electronic engineering. Experience in digital PCB design and digital electronics norms, laws, and standards required.

Provide statistical consultation on clinical trial design and analysis across multiple development stages and therapy areas. Develop and implement innovative statistical approaches, including model-based methods. Communicate complex quantitative topics clearly for diverse audiences. Contribute to scientific publications and industry initiatives.

This role contributes to the design and delivery of a biologics manufacturing facility, ensuring compliance with regulatory and quality requirements. The Qualification and Validation Lead will define and represent qualification and validation requirements, review technical documentation, and support audits and regulatory interactions.

Downstream Biomanufacturing Process Expert needed for a biologics manufacturing project. Will represent manufacturing needs, translate operational requirements, and ensure the future facility is designed for safe, high-quality, and efficient production. Requires a degree in a relevant field, experience in biopharmaceutical operations, and strong knowledge of mammalian biopharmaceutical production. Fluent in English, occasional travel to the US may be required.

Leads quality function for products, ensuring compliance with legal, regulatory, and customer requirements. Manages QA/QC procedures, inspection methods, and supplier quality. Provides quality leadership, technical expertise, and coaching to Quality teams.

Lead multidisciplinary System Architecture activities across Solution, Requirements & Verification, Interface Definition & ConOps functions. Provide technical leadership and direction to SE teams supporting complex aerospace and defense programs. Manage system architecture, interface control, requirements development, verification & validation, and technical trade studies.

Senior Product Manager to lead strategy, roadmap, and lifecycle of Graykey, a strategic product line in digital forensics. Responsibilities include translating customer and business needs into product vision, collaborating with cross-functional teams, and driving product integration efforts. Requires 5+ years of experience in product management, strong customer empathy, and excellent communication and collaboration skills.

Commercial Alliance Manager needed with 5-8 years of experience in alliance management, technology sales, or business development. Proven track record of revenue growth through alliances required. Excellent communication and presentation skills essential. Must be a self-starter with the ability to work independently and collaboratively. Willingness to travel up to 30%.

Install and maintain advanced medical technology, including high-energy accelerator components, at customer locations worldwide. Troubleshoot complex systems, provide on-site support, and train colleagues. Requires a Master's degree in electro-mechanics or equivalent experience and proven expertise in root-cause analysis. Strong communication and interpersonal skills are essential. Willingness to travel up to 60% of the time, including weekends, is required.

Steer monthly, quarterly, and annual consolidation under IFRS. Prepare group statutory financial statements and quarterly reporting. Manage and optimize the consolidation system.